Allele Registry

Canonical Allele Identifier: PA124212

Gene: INSR HGNC NCBI

ClinVar RCV:

RCV000015793

ClinVar Variation:

14679

HGVS (amino-acid)	Matching Registered Transcripts
NP_001073285.1:p.Gly1023Val	CA124211 NM_001079817.3:c.3068G>T